Canonical Allele Identifier: CA377673439
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942341G>A , CM000672.2:g.94942341G>A GRCh38
NC_000010.10:g.96702098G>A , CM000672.1:g.96702098G>A GRCh37
NC_000010.9:g.96692088G>A NCBI36
NG_008385.1:g.8684G>A
NG_008385.2:g.9184G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.481G>A MANE Select ENSP00000260682.6:p.Ala161Thr
ENST00000643112.1:c.481G>A ENSP00000496202.1:p.Ala161Thr
ENST00000645207.1:n.634G>A
ENST00000260682.6:c.481G>A ENSP00000260682.6:p.Ala161Thr
ENST00000461906.1:n.506G>A
ENST00000473496.1:n.252G>A
NM_000771.3:c.481G>A NP_000762.2:p.Ala161Thr
NM_000771.4:c.481G>A MANE Select NP_000762.2:p.Ala161Thr